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    <br/>第九章 DNA催化与肽展计算和AOPM-TXH-VECS-IDUQ元基解码
    <br/>The DNA Catalytic & PDE Computing and The Derivation of New TXH
    Initons DNA
    <br/>催化 与 肽展计算 和 AOPM-TXH-VECS-IDUQ 元基解码 013026 中文
    <br/>罗瑶光
    <br/>
    <br/>观点: 1: 解放生产力, 创造新的生产力. 2: 优化已有的生产工具更好的适应生产环境. 3:
    更好的辅助智慧生物 理解, 适应和 改造环境; 医学教育领域实践, 商品与 API 需求分解;
    DNA 与神经元函数 肽展编码, 类人与进化系统设计. 关键词: 元基, 肽展公式, 黄嘌呤,
    次黄嘌呤, 2 氨基腺嘌呤, 触发, 探索, 嘌呤弧, 碱基对, 催化神经网络引言: 在 DNA 编码
    与 肽计算定理公式 推导出来后, 作者 根据变嘧啶定义 顺藤摸瓜 通过肽计算来 反演推导DNA
    编码的存在性和 解码真实性, 于是又有了些新发现, 如 TX-H-U 活泼元基在 DNA 催化计算的
    准确定义, 和元基在 生化计算环境中 的存在模型. 这些新发现 将在这篇文章细节中
    一一阐述:目录:

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    <br/>1. 推导与定义:甲基胞嘧啶在DNA编码和肽计算中具体定义为IDUQ-U变嘧啶

    <br/>
    <br/>下述文字不仅阐述了 IDUQ 应激元基中的变嘧啶存在形式和参与催化计算的方式,
    作者通过论证找到了它真实存在形态. 和在 DNA 中具体应用功能和定义. 肽展公式, 智慧性元基
    , 多样性元基, 应激性元基, 遗传核酸, 变嘧啶, 嘧啶, 嘌呤, 甲基胞嘧啶.
    <br/>
    <br/>自从德塔 AOPM VECS IDUQ 的 DNA 意识编码 1. 2. 2 体系出来后, 我一直在思考
    怎么进行单链化, 在 肽展公式 1. 2. 2 推导 出来后, 我很惊讶, DNA 竟然可以展开成一篇
    文章, 我得到很多新奇的发现, 同时, 我还推出了变嘧啶 这个 莫须有的东西, 在不断的 推导
    和模拟我的语义词汇时候, 我发现, 变嘧啶成了不可缺失的组成部分. 于是觉得 有必要进行理论化
    的进行描述这个 莫须有的物质客观上是否真的存在. 是否有 合理性的分子表达式. 因为主观上
    变嘧啶是 IDUQ 中的 U, DNA 和肽计算不可缺少的一个核心微元基单位.
    <br/>
    <br/>L pyrimidine Initon. 为了很好的描述这个 变嘧啶, 我开始观察 尿 嘧啶, 胞嘧啶
    , 鸟嘌呤, 腺嘌呤, 胸腺嘧啶, 在人卫九的 生物化学与分子生物学中第 32 页 核苷酸嘌呤嘧啶
    结构式, 第 39 页, TAT 和 第 46 页 tRNA 以及 59 页 酶的给工作原理, 于是我首先确定
    嘧啶结构 如图 第 11 处, 我得到一个 通用嘧 啶结构. 在肽展公式推导中, 我已经有了比较
    具体的完整的 逻辑公式, 比如 C = U +D, D = DD, S = I +Q, C = D, I = U, 我开始
    持续的绝对专注, 我只能依靠这些公式来推导 变嘧啶. 通过图片, 推导出 11 和 6, 7, 8,
    我思考了下, 氨基 对上进行 5 碳环肽解, 腺嘧啶需要 共价氧, 那 鸟嘌呤元基 C 上的公共价氧
    应该对应的 UD 一定需要胺基来维 持 DNA 平衡, 于是得到 9 和 10, 我不确定 10 的
    第五个位置的氮是共价 NH, 还是不共价 NH2, 于是开始继续思 考. 非常的幸运, 按照数字逻辑
    和离散数学 补码原理 推导 见 肽展公式 1. 2. 2 国家论著, 我得到了 C = D 这个公 式,
    同时又得到 C = U + D 这个公式, 于是我不妨大胆一点, U 应该类似 D, 变嘧啶应该类似
    胞嘧啶的结构. 于是确定 苯环上第 5 位的氮应该是 共价存在. 于是得到了 13 的 嘧啶物质.
    我又迷惑了 13 不就是 胞嘧啶吗? 我思考了 下, I = U, 我还有这个公式, 尿嘧啶推导
    变嘧啶, 可是 13 是胞嘧啶呀. 开始疑惑了我的肽展公式有 问题? 我一直 在思考, I = U,
    U 和 胞嘧啶一样, 如果确定我的公式是正确的, 那我只有一个答案, 就是 U 包含 胞嘧啶.
    结构 于是 我又看了下 胸腺嘧啶的甲基, 又看了下 胞嘧啶++ 酸化成尿嘧啶, 我得到一种思路,
    难道 尿嘧啶 通过碱化可得 到一种包含胞嘧啶分子结构的氨基嘧啶? 氢氧化钠? 不, 那是烧碱,
    烈着呢, 甲烷? 甲烷有可能,
    <br/>
    <br/>想起浏阳三中的罗满生老师当年教这堂课, 我又开始思考, 我来了些灵感, 人体的组织液里面
    细胞核裂变怎么会有甲烷和烧碱呢? 除了胃和 放屁, 有甲烷, 硫铵,. .. 硫铵,, , 氨碱?
    难道是氨基碱? 尿嘧啶 与氨基碱类, 可以得到 15 类 一大把 胞嘧 啶族的分子, 我又看了下
    胸腺嘧啶的甲基, 难道是氨碱? NH2CH3 ? 这就对上号了, 最终我的得到, 15 这个物质, 因为,
    人体组织液里不可能会有强碱分子的, 所以, 氨基碱类这种弱碱性普遍存在的组织液里, 尿嘧啶可以被氨化
    重复利用参与核计算.
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    <br/>小结论:
    <br/>
    作者归纳通过计算逻辑推导, 如 Figure1 的第 15 处, 甲基胞嘧啶 的客观真实存在
    在微分催化中执行变嘧啶的改元基逻辑. 作者用姓氏的首字母命名为变嘧啶 L-Pyrimidine.
    <br/>
    <br/>
    The Definition of The Methylcytosine in DNA Catalytic Computing
    and The Derivation of The IDUQ-U of The L-Pyrimidine
    <br/>
    <br/>
    Since The 'AOPM VECS IDUQ and The Initons Catalytics were
    Reflected Between Humanoid DNA and Nero Cell 1.2.2' finished. The
    author has been thinking about how to let the software programming
    code, was built as the AOPM VECS IDUQ linklist. Until the
    'AOPM-VECS-IDUQ Catalytic Initons PDE LAW and Its Application1.2.2'
    finished. Human began to know that the DNA could be extended for an
    article. At the same time, the author did research out a lot of
    results. For example, L-Pyrimidine. Because of the large derivations
    and simulations from the human thinking and mind cognitions. It proved
    that L-pyrimidine became an important part of the NLP and DNA catalytic
    computing. Then the author began to prove that 'Does the L-pyrimidine a
    real thing in this real world?'. 'Does the L-pyrimidine which has Its
    own chemical mode?'. Since we had AOPM VECS IDUQ, the U/update was one
    of a basic Initon, not only the U/update Initon was an important part
    of the DNA catalytic computing. It also was a basic part of the PDN
    extension Initons. L pyrimidine Initon. At the first, the author named
    It as L-pyrimidine Initon, the first char of 'Luo', 'Liang', 'Li' and
    'Liu'. (Author's family). Since he had Uracil, Cytosine, Guanine,
    Adenine and Thymine. From the Biochemistry and Molecular Biology, page
    32, It showed the chemical mode of the Purines and Pyrimidines. From
    the page 39, page 46 and page 59, It showed the TAT, tRNA, and Enzyme
    tasks. So, the author did a definition of a common structure of
    Pyrimidine. The author did an identification with a figure 11 at the
    picture:
    https://gitee.com/DetaChina/collection-of-papers-by-deta/blob/master/lpyrimidine1.jpg.
    <br/>
    <br/>
    Since we had already got a DNA PDE formula for C= U+ D, D= DD, S=
    I+ Q, C= D and I= U etc. Ok let's continue, according to those
    formulas, author could find out the 11, 6, 7, 8 factors in the
    picture1. It showed for the Amino pair. Adenine and Thymine needed a
    covalent oxygen. Also, Cytosine and Guanine need Amino base, the author
    proved the DNA catalytic computing absolutely was an accumulation of
    PLC digital logic computing. The 'Covalent Oxygen' and 'Amino base' was
    the DNA clock. Base from the human heart beats. There fore, it showed
    the results of 9 and 10, For the position of 5, which was NH or NH2,
    the author began to fall in thinking. From the 'Catalytic Initons PDE
    law and Its Application's formula', It had C= D, C= U+ D, then could
    get U-> D. The mode of L-pyrimidine will similar with Sytosine. Above
    all, it proved that the position of 5, of the Pyrimidine was a covalent
    Nitrogen. As the figure of 13. Definitely, the figure 13 was Sytosine.
    Please see the I= U formula. The Uracil could be an L-pyrimidine, but
    L-pyrimidine was similar with Sytosine. If the PDE formula was a true
    function and the L-pyrimidine was not the same with Sytosine, then
    proved L-pyrimidine, which contained Sytosine. Finally seen the
    Thymine, the CH3 with the position of 1, the author thought, NH2-CH3,
    which added Uracil, could be a Methylcytosine. Because scientist was
    hard to find NaOH, CH4. In human's tissue fluid, only the result that
    was NH2-CH3 or an Amino Alkali. Finally, author proved the figure 15,
    Methylcytosine was an L-pyrimidine.
    <br/>
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